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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Alliance of Genome Resources
Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
| Source | Last Updated |
|---|---|
| Alliance of Genome Resources | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▼ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0050967 | spinocerebellar ataxia type 17 | HGNC:11588 | Homo sapiens (human) | 6908 | TBP |
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| DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:12241 | beta thalassemia | HGNC:4827 | Homo sapiens (human) | 3043 | HBB |
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| DOID:0080324 | tuberous sclerosis 1 | HGNC:12362 | Homo sapiens (human) | 7248 | TSC1 |
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| DOID:10652 | Alzheimer's disease | HGNC:7782 | Homo sapiens (human) | 4780 | NFE2L2 |
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| DOID:12347 | osteogenesis imperfecta | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:5844 | myocardial infarction | HGNC:9052 | Homo sapiens (human) | 5328 | PLAU |
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| DOID:10487 | Hirschsprung's disease | RGD:2536 | Rattus norvegicus (Norway rat) | 50672 | Ednrb |
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| DOID:0111077 | pyruvate kinase deficiency of red cells | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:4535 | hypotrichosis | RGD:735015 | Rattus norvegicus (Norway rat) | 291754 | Dsg4 |
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| DOID:6432 | pulmonary hypertension | HGNC:11050 | Homo sapiens (human) | 6532 | SLC6A4 |
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| DOID:10763 | hypertension | HGNC:9236 | Homo sapiens (human) | 5468 | PPARG |
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| DOID:9255 | frontotemporal dementia | HGNC:6893 | Homo sapiens (human) | 4137 | MAPT |
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| DOID:0050879 | fragile X-associated tremor/ataxia syndrome | HGNC:3775 | Homo sapiens (human) | 2332 | FMR1 |
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| DOID:10907 | microcephaly | HGNC:19048 | Homo sapiens (human) | 259266 | ASPM |
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| DOID:14179 | X-linked agammaglobulinemia | HGNC:1133 | Homo sapiens (human) | 695 | BTK |
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| DOID:2749 | glycogen storage disease Ia | HGNC:4056 | Homo sapiens (human) | 2538 | G6PC1 |
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| DOID:9970 | obesity | HGNC:24678 | Homo sapiens (human) | 79068 | FTO |
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| DOID:10584 | retinitis pigmentosa | HGNC:10012 | Homo sapiens (human) | 6010 | RHO |
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| DOID:384 | Wolff-Parkinson-White syndrome | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:2217 | Bernard-Soulier syndrome | HGNC:4439 | Homo sapiens (human) | 2811 | GP1BA |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:4010 | Homo sapiens (human) | 2521 | FUS |
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| DOID:10763 | hypertension | RGD:3001 | Rattus norvegicus (Norway rat) | 24536 | Lepr |
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| DOID:1064 | cystinosis | HGNC:2518 | Homo sapiens (human) | 1497 | CTNS |
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| DOID:12134 | factor VIII deficiency | HGNC:3546 | Homo sapiens (human) | 2157 | F8 |
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